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Molzym Genomoc DNA Isolation

 

Bedefits:

High DNA yield   |   High DNA quality   |   Simple handlinf   |   Low hands-on-time   |   Easy processing of viscous extracts

The PrestoSpin D Mini spin column isolation kits are available for the isolation of genomic DNA from a variety of samples: i) Grown microorganisms, including bacteria, yeasts and filamentous fungi, ii) cultured human and animal cells, and iii) whole blood from humans and animals. Molzym’s proprietary technology, Cation Complexation Technology (CCT), guarantees easy handling, low hands-on time, extremely high yields and high quality standards. The porosity and outstanding binding capacities of Molzym's special matrices allow the passage of even highly viscous extracts without retention and the isolation of unmet quantities of DNA.

Kits - Genomic:

Mini spin kits are supplied for the purification of genomic DNA. Extraction can be performed from grown bacteria, PrestoSpin D Bug, and fungi, PrestoSpin D Fungi. Genomic DNA can be purified from whole blood and cutured eukaryotic cells using the PrestoSpin D Blood&Cell kit.

Productinformation:

Product OrderNr. Size Price Shop
PrestoSpin D Blood & Cell
Sample: blood and cell culture
Max.Volume: 0.2 ml / 107 cultured cells
D-090-050 50 React. 85,-
D-090-250 250 React. 383,-
PrestoSpin D Bug
Sample: Gram-positive/ Gram-negative bacteria
Max.Volume: 5 ml ( up to 2 x 1010 E.coli cells)
D-040-050 50 React. 99,-
D-040-250 250 React. 419,-
PrestoSpin D Fungi
Sample: Yeasts and fungi
Max.Volume: 2 ml or 250 mg wet wt. mycelium
D-050-050 50 React. 99,-
D-050-250 250 React. 419,-

Technology - Genomic:

Key Features:

  • pH independent
  • extremly high binding capacity
  • suitable for viscous material
  • no shearing forces

CCT – High yield nucleic acid purification technology

Molzym’s proprietary technology allows the purification of large amounts of highly pure DNA. The CCT technology explores the binding of DNA to special matrices in the presence of magnesium ions. After the initial binding of DNA, impurities like proteins, metabolites and salts are removed by two short washing steps. Finally, the bound nucleic acids are eluted with a buffer removing the magnesium ions by using low EDTA concentration (TE buffer). CCT and the Molzym matrices guarantee a high binding capacity of the mini spin columns. The high porosity of Molzym matrices let highly viscous samples pass the column smoothly thus reducing shearing forces and hence resulting in high molecular size DNA.

 

ahn

brand

eppendorf

gilson

mettler toledo

heidolph

neolab

satorius

systec

thermo scientific

zeiss